MEDICS CHOICE LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution 
K.C. Pharmaceuticals, Inc.

----------

Medics Choice Lubricant Eye Drops 0.4mL 5ct. (PLD)

Active ingredients

carboxymethylcellulose sodium 0.5%

Purpose

Carboxymethylcellulose sodium......Lubricant

Uses

Warnings

For external use only

Do not use this product if

  • solution changes color or becomes cloudy

When using this product

  • do not reuse
  • once opened, discard
  • to avoid contamination, do not touch tip of container to any surface
  • do not touch unit-dose tip to eye

Stop use and ask a doctor if

  • you experience eye pain
  • changes in vision occur
  • redness or irritation of the eye continues
  • redness or irritation of the eye worsens or persists for more than 72 hours

Keep out of the reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

Other information

Inactive ingredients

calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.

**may contain these ingredients to adjust pH.

CARTON

MEDICS CHOICE LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55651-030
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYDROCHLORIC ACID (UNII: QTT17582CB)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55651-030-015 in 1 CARTON02/10/2020
10.4 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01802/10/2020
Labeler - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIBusiness Operations
K.C. Pharmaceuticals, Inc.174450460manufacture(55651-030) , pack(55651-030) , label(55651-030)

Revised: 12/2023
Document Id: 0d29b49a-71d6-b6b9-e063-6294a90a9247
Set id: 9ddfc275-602f-413b-e053-2995a90a11cb
Version: 3
Effective Time: 20231223
 
K.C. Pharmaceuticals, Inc.